4.7 Article

Gold Nanobeads with Enhanced Absorbance for Improved Sensitivity in Competitive Lateral Flow Immunoassays

Journal

FOODS
Volume 10, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/foods10071488

Keywords

gold nanobeads; lateral flow immunoassay; enhanced sensitivity; mycotoxin; corn sample

Funding

  1. National Key Research and Development Program of China [2018YFC1602505]
  2. National Natural Science Foundation of China [32001788]
  3. Interdisciplinary Innovation Fund of Natural Science, Nanchang University [9166-27060003-ZD01]
  4. Opening Fund of Jiangsu Key Laboratory for Food Quality and Safety-State Key Laboratory Cultivation Base, Ministry of Science and Technology [028074911709]

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The study enhances the detection sensitivity of lateral flow immunoassay (LFIA) by synthesizing three different sizes of gold nanobeads (GNBs), with the 129 nm GNBs showing the best sensitivity for fumonisin B-1 (FB1) detection. The developed GNB-LFIA demonstrates improved performance compared to conventional LFIA based on 20-40 nm AuNPs.
Background: Colloidal gold based lateral flow immunoassay (LFIA) commonly suffers from relatively low detection sensitivity due to the insufficient brightness of conventional gold nanoparticles (AuNPs) with the size of 20-40 nm. Methods: Herein, three kinds of gold nanobeads (GNBs) with the size of 94 nm, 129 nm, and 237 nm, were synthesized by encapsulating numerous hydrophobic AuNPs (10 nm) into polymer matrix. The synthesized GNBs exhibited the enhanced colorimetric signal intensity compared with 20-40 nm AuNPs. The effects of the size of GNBs on the sensitivity of LFIA with competitive format were assessed. Results: The results showed that the LFIA using 129 nm GNBs as amplified signal probes exhibits the best sensitivity for fumonisin B-1 (FB1) detection with a cut-off limit (for visual qualitative detection) at 125 ng/mL, a half maximal inhibitory concentration at 11.27 ng/mL, and a detection limit at 1.76 ng/mL for detection of real corn samples, which are 8-, 3.82-, and 2.89-fold better than those of conventional AuNP40-based LFIA, respectively. The developed GNB-LFIA exhibited negligible cross-reactions with other common mycotoxins. In addition, the accuracy, precision, reliability, and practicability were demonstrated by determining real corn samples. Conclusions: All in all, the proposed study provides a promising strategy to enhance the sensitivity of competitive LFIA via using the GNBs as amplified signal probes.

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